Difference between revisions of "LII:LIMSpec for Cannabis Testing"

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:[[LII:LIMSpec for Cannabis Testing/Closing remarks|6. Closing remarks]]
:[[LII:LIMSpec for Cannabis Testing/Closing remarks|6. Closing remarks]]
::Putting LIMSpec for Cannabis Testing to use
::Putting those requirements to practical use


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[[Category:LII:Guides, white papers, and other publications]]
[[Category:LII:Guides, white papers, and other publications]]

Latest revision as of 01:14, 4 January 2024

GreenChemicals.jpg

Title: LIMSpec for Cannabis Testing

Edition: 2023

Author for citation: Shawn E. Douglas

License for content: Creative Commons Attribution-ShareAlike 4.0 International

Publication date: June 2023

Many specification documents for laboratory informatics systems have been compiled over the years. Most of them tend to focus on a potential client's "wishlist" of features for a given system. This industry-specific version of the base LIMSpec document is different; it attempts to take a regulatory-, standards-, and guidance-based approach to building a specification document for laboratory informatics systems used within the cannabis testing laboratory. After the introduction, methodology, and a discussion of industry-specific functionality requirements, cannabis testing-related LIMSpec requirements are organized and listed, in all but a few cases supported by one or more regulations, standards, or guidance documents. This guide also addresses the functionality requirements specific to cannabis testing, matching them to entries in the specification. New in the 2023 edition is a Microsoft Word version of the specification, for download and use in the last chapter.

The table of contents for LIMSpec for Cannabis Testing is as follows:

1. Introduction
Introduction and methodology
LIMS functionality requirements specific to cannabis testing
2. Primary laboratory workflow
1. Sample and experiment registration
2. Sample management
3. Core laboratory testing and experiments
4. Results review and verification
5. Sample, experiment, and study approval and verification
6. Reporting
3. Maintaining laboratory workflow and operations
7. Document and records management
8. Personnel and resource management
9. Compliance management
10. Instrument and equipment management
11. Batch and lot management
12. Scheduled event management
13. Instrument data capture and control
14. Standard and reagent management
15. Inventory management
16. Investigation and quality management
4. Technology and performance improvements
17. Instrument data systems functions
18. Systems integration
19. Laboratory scheduling and capacity planning
20. Lean laboratory and continuous improvement
21. Artificial intelligence and smart systems
5. Security and integrity of systems and operations
22. Data integrity
23. Configuration management
24. System validation and commission
25. System administration
26. Cybersecurity
27. Information privacy
6. Closing remarks
Putting those requirements to practical use